Mistletoe Therapy in Primary and Recurrent Inoperable Pancreatic Cancer

NCT02948309 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 290

Last updated 2023-01-13

No results posted yet for this study

Summary

In this study a mistletoe preparation (Iscador Qu) is added to standard therapy in inoperable pancreatic cancer in order to evaluate effect on overall survival and health-related quality of life. Half of participants will take subcutaneous injections with mistletoe in addition to standard therapy (palliative chemotherapy or best supportive care); the other half will receive a placebo and standard therapy.

Conditions

Interventions

DRUG

Mistletoe extract (Iscador Qu)

1ml subcutaneous injection 3 times/week, dose escalation 0,01mg - 20mg

DRUG

Placebo

1ml subcutaneous injection 3 times/week

Sponsors & Collaborators

  • University of Witten/Herdecke

    collaborator OTHER
  • Karolinska Institutet

    collaborator OTHER
  • Regional Cancer Centre Stockholm Gotland

    collaborator OTHER
  • Stiftelsen Konung Gustaf V:s Jubileumsfond för cancerforskning

    collaborator UNKNOWN
  • Signe & Ane Gyllenbergs Stiftelse

    collaborator UNKNOWN
  • Ekhagastiftelsen

    collaborator OTHER
  • Dagmar Ferbs Minnesfond

    collaborator UNKNOWN
  • Cancerforskningsfonden i Norrland

    collaborator UNKNOWN
  • Immunpathologisches Labor, University Tübingen

    collaborator UNKNOWN
  • The Sjöberg Foundation

    collaborator UNKNOWN
  • Karolinska University Hospital

    lead OTHER

Principal Investigators

  • Annika Bergquist, Ass Prof · Gastrocentrum Karolinska University Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-06-30
Primary Completion
2022-09-30
Completion
2022-09-30

Countries

  • Sweden

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02948309 on ClinicalTrials.gov